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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13282생성일: 2026년 10월 24일

Iodoacetamide → 2-(2-(6-(4-Fluoro-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-acetamide

https://huagongshe.com/ko/reaction/13282

반응식

참여 물질

역할이름HCID투입량
반응물IodoacetamideHCID 3727—
반응물Potassium CarbonateHCID 11430—
반응물5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazoleHCID 23145575—
용매AcetonitrileHCID 6342—
생성물2-(2-(6-(4-Fluoro-phenoxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-acetamideHCID 23145124—

반응 단계

11.4 mg of potassium carbonate and 11.1 mg of iodoacetamide were added in order to an acetonitrile (1 ml) solution of 20 mg of 5-(4-fluoro-phenoxy)-2-pyridin-2-yl-6-pyrrolidin-2-yl-1H-benzimidazole obtained in Example 168, and the reaction liquid was stirred overnight at room temperature. The reaction liquid was concentrated, and the resulting residue was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid], and the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline in order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-82f3e1f2420e4be1992565f49031ff26
출처 메모uspto-grants-2010_06